Recall: Platinum 40000 Aphrodisiac Capsules
On 2019-04-09, the FDA announced that SD Import is conducting a recall on Aphrodisiac Capsules due to possible undeclared undeclared sildenafil. The recalled products were sold under the brand name(s) Platinum 40000 during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 6 drugs recalls due to potential undeclared ingredients, including ground kopi jantan tradisional natural herbs coffee, dietary supplement and more. Additionally, there have been 20 drug and medical device recalls due to other health hazards as well as 67 food recalls.
Company Contact Information:
Name: SD Import
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Aphrodisiac Capsules
Brand Name(s): Platinum 40000
Reason for Recall: Undeclared Sildenafil
Official Recall Date: 2019-04-09
Additional information provided by the FDA.gov:
SD Import, LLC is voluntarily recalling all lots of Aphrodisiac, Capsules to the consumer level. The products have been found to be tainted with sildenafil. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an active pharmaceutical ingredient in FDA approved product used in the treatment of erectile dysfunction. The presence of sildenafil in Aphrodisiac capsules renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.